A kind of hierarchical structure coating separator for lithium-sulfur battery and preparation method thereof
A hierarchical structure, lithium-sulfur battery technology, applied in the direction of lithium batteries, structural parts, secondary batteries, etc., can solve the problems that the physical mixing of various materials cannot be completely uniform, increase the material preparation process and application costs, and make it difficult to contribute to electronic pathways, etc. , to achieve the effects of green and environmentally friendly large-scale production, improved electrochemical performance, and easy large-scale production
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Embodiment 1
[0052] (1) Dissolve 1.354g of manganese acetate and 0.952g of benzoic acid as reaction substances in 40mL of diethylformamide, stir for 10h until completely dissolved, then add 1.295g of terephthalic acid and stir to dissolve;
[0053] (2) hydrothermal reaction at 200°C for 6 hours in a closed environment, and then naturally cooled to room temperature to obtain the reaction product;
[0054] (3) The reaction product was filtered to obtain a white solid, washed with distilled water and ethanol until the pH was neutral, and vacuum-dried and dehydrated at 60° C. for 24 hours to obtain a manganese-based coordination polymer;
[0055] (4) Heating the manganese-based coordination polymer to 600°C at a heating rate of 3°C / min in an argon atmosphere, keeping it for 2 hours and then cooling to obtain the MnO / C precursor;
[0056] (5) The MnO / C precursor was heated to 1000°C at a rate of 3°C / min in a nitrogen atmosphere with a purity of 99.9% (volume fraction), kept for 2 hours and then...
Embodiment 2
[0061] (1) Dissolve 1.354g of manganese acetate and 1.904g of benzoic acid as reaction substances in 40mL of diethylformamide, stir for 24 hours until completely dissolved, then add 2.59g of terephthalic acid and stir to dissolve;
[0062] (2) Hydrothermal reaction at 200°C for 12 hours in a closed environment, and then naturally cooled to room temperature to obtain the reaction product;
[0063] (3) The reaction product was filtered to obtain a white solid, washed with distilled water and ethanol until the pH was neutral, and vacuum-dried and dehydrated at 70°C for 24 hours to obtain a manganese-based coordination polymer;
[0064] (4) Heating the manganese-based coordination polymer to 600°C at a heating rate of 5°C / min in an argon atmosphere, keeping it for 2 hours and then cooling to obtain a MnO / C precursor;
[0065] (5) Heating the MnO / C precursor in a nitrogen atmosphere with a purity of 99.9% (volume fraction) to 1000°C at a heating rate of 5°C / min, keeping it for 2 ho...
Embodiment 3
[0070] (1) Dissolve 1.354g of manganese acetate and 1.904g of benzoic acid as reaction substances in 60mL of dimethylformamide, stir for 30h until completely dissolved, then add 3.885g of terephthalic acid and fully stir to dissolve;
[0071] (2) Hydrothermal reaction at 180°C for 10 hours in a closed environment, and then naturally cooled to room temperature to obtain the reaction product;
[0072] (3) The reaction product was filtered to obtain a white solid, washed with distilled water and ethanol until the pH was neutral, and vacuum-dried and dehydrated at 100°C for 20 hours to obtain a manganese-based coordination polymer;
[0073] (4) Heating the manganese-based coordination polymer to 550°C at a heating rate of 5°C / min in an argon atmosphere, keeping it for 3 hours and then cooling to obtain a MnO / C precursor;
[0074] (5) The MnO / C precursor was heated to 1100°C at a rate of 5°C / min in a nitrogen atmosphere with a purity of 99.9% (volume fraction), kept for 2 hours and...
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